Canonical Allele Identifier: CA2366533195

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129027A= , CM000682.2:g.46129027A=	GRCh38
NC_000020.10:g.44757666A= , CM000682.1:g.44757666A=	GRCh37
NC_000020.9:g.44191073A=	NCBI36
NG_007279.1:g.15761A= , LRG_40:g.15761A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.904A=	ENSP00000512096.1:n.904A=
ENST00000695675.1:n.2697A=
ENST00000372285.8:c.821A= MANE Select	ENSP00000361359.3:p.Gln274=
ENST00000372276.7:c.*147A=	ENSP00000361350.3:n.*147A=
ENST00000372285.7:c.821A=	ENSP00000361359.3:p.Gln274=
ENST00000466205.5:c.723A=
ENST00000489304.5:n.897A=
ENST00000620709.4:c.*368A=	ENSP00000484074.1:n.*368A=
NM_001250.5:c.821A=	NP_001241.1:p.Gln274=
NM_001302753.1:c.*147A=	NP_001289682.1:n.*147A=
NM_152854.3:c.*147A=	NP_690593.1:n.*147A=
NR_126502.1:n.914A=
XM_005260617.2:c.833A=	XP_005260674.1:p.Gln278=
XM_005260619.2:c.677A=	XP_005260676.1:p.Gln226=
XR_936660.1:n.821A=
NM_001322421.1:c.833A=	NP_001309350.1:p.Gln278=
NM_001322422.1:c.665A=	NP_001309351.1:p.Gln222=
NM_001362758.1:c.*147A=	NP_001349687.1:n.*147A=
NR_136327.1:n.817A=
XM_005260619.3:c.677A=	XP_005260676.1:p.Gln226=
XM_017028135.1:c.856A=	XP_016883624.1:p.Arg286=
XM_017028136.1:c.754A=	XP_016883625.1:p.Arg252=
NM_001250.6:c.821A= MANE Select	NP_001241.1:p.Gln274=
NM_001302753.2:c.*147A=	NP_001289682.1:n.*147A=
NM_001322421.2:c.833A=	NP_001309350.1:p.Gln278=
NM_001322422.2:c.665A=	NP_001309351.1:p.Gln222=
NM_001362758.2:c.*147A=	NP_001349687.1:n.*147A=
NM_152854.4:c.*147A=	NP_690593.1:n.*147A=
NR_126502.2:n.854A=
NR_136327.2:n.757A=